医学
曲美替尼
外显子
肿瘤科
肺癌
内科学
临床试验
临床研究阶段
癌症研究
MAPK/ERK通路
遗传学
基因
激酶
生物
作者
Matthew S Lara,Jonathan W. Riess,Jonathan W. Goldman,Fei Jiang,Trever G. Bivona,Collin M. Blakely
标识
DOI:10.1016/j.cllc.2024.07.002
摘要
MET tyrosine kinase inhibitor (TKI) therapy is associated with improved outcomes in patients with nonsmall cell lung cancer (NSCLC) harboring a MET alteration, including MET exon 14 (METex14) skipping mutation, MET amplification, or MET fusion. However, primary or acquired resistance to TKI therapy ultimately develops. In preclinical models, hyperactivation of MAPK signaling was shown to promote resistance to MET TKI; resistance was overcome by co-treatment with a MET inhibitor and a MEK inhibitor. This phase I/Ib study offers a potential combination strategy simultaneously targeting MET (with capmatinib) and MEK signaling (with trametinib) to overcome resistance to MET inhibitor monotherapy in METex14 NSCLC.
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